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HRID 247747作成日:2026年10月26日

Hexane → N-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethylpropanamide

https://huagongshe.com/reaction/247747

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Ethenamine, 2-phenyl-HCID 155076—
反応物2,2,2'-TrimethylpropionanilideHCID 2734005—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物N-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethylpropanamideHCID 1096893778%

反応手順

A stirred solution of N-[(2-methyl)phenyl]-2,2-dimethylpropanamide (95.6 g, 0.5 mol) in THF (500 ml, dried over 4 Å molecular sieves) was cooled to 0° C. and treated with 1.6M n-butyllithium in hexane (630 ml, 1.0 mol). The addition of n-butyllithium was complete after 45 minutes. During the addition, the temperature of the mixture was maintained below 10° C. with external cooling. The resultant dianion solution was aged (about 1-2 hrs) at 0° C. until the homogeneous orange solution became a white heterogeneous slurry. The dianion was then quenched with N-benzylidenemethylamine (63.7 g, 0.6 mol) and aged for 30 minutes at 15°-25° C. The reaction mixture was diluted with ether (200 ml), treated with crushed ice (200 g), and stirred for 15 minutes. The organic phase was separated, washed with saturated sodium chloride, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residual oil was crystallized from hexane (400 ml) at 5° C. to give N-[2-(2-methylamino-2-phenylethyl)phenyl]-2,2-dimethylpropanamide (121.2 g, 0.39 mol) in 78% yield. The product had a melting point of 85°-86° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04709093
出典データセットuspto-grants-1987_11
ORD IDord-2719aa70f12b4ba4b2d8f113f5f3a760
出典メモuspto-grants-1987_11